Methods for treatment of inflammatory and infectious diseases

ABSTRACT

Methods and therapeutic treatments of diseases such as viral infections are provided including applying peg-Arginase I. Methods are provided that treat inflammation mediated diseases with peg-Arginase I.

CROSS-REFERENCE TO RELATED APPLICATIONS

The present disclosure is a continuation-in-part of U.S. patent application Ser. No. 13/828,669, entitled “Methods for Treatment of Ocular Diseases” filed on Mar. 14, 2013, which application claims benefit of U.S. Provisional Application 61/664,464 filed Jun. 26, 2012, all of which are incorporated herein by reference.

STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT

This invention was made with government support under grants P20RR021970 and P20GM103501 awarded by the National Institutes of Health. The government has certain rights in the invention.

FIELD

The present disclosure relates generally to treatment of diseases. More particularly, in exemplary though non-limiting embodiments, the present disclosure relates to therapeutic methods to treat viral infections and inflammation mediated diseases.

BACKGROUND

Viral diseases are caused by a combination of virus-mediated cytopathic effects and an acutely overactive (cytokine storm) or chronic inflammatory response. The immune response, intended to control the infection, frequently exacerbates the disease and causes complications, such as blindness (viral stromal keratitis), encephalitis (West Nile virus infections), acute respiratory distress syndrome (pandemic influenza) and even death. Effective anti-viral drugs in general do not prevent inflammatory complications and therefore, corticosteroids are frequently required. However, steroids can exacerbate viral replication resulting in a difficult to interrupt vicious cycle where viral replication and inflammation cannot be controlled at the same time and in the end result in severe damage of the tissues. Accordingly, there is need for improved therapies that may be able to control viral replication and inflammation simultaneously and therefore prevent damage to the tissues.

Improved therapies to control viral replication and information have potential application in severe viral infections of the eye. The cornea is the highly transparent outer-most layer of the eye that provides a large portion of the eye's refractive power and shields against infection by pathogens. Since even the smallest of cells can affect visual acuity, normal corneal tissue lacks all vasculature and is immunologically privileged to reduce influx of inflammatory cells. Generally, in the absence of ocular disease and/or trauma, the lack of vasculature and inflammatory response of the cornea ensures visual acuity is maintained. However, under certain ocular situations, the lack of vascularization and/or suppressed inflammatory response may be compromised.

For example, trauma to the eye by a foreign object (e.g. dust, sand, or mechanical), a surgical procedure (e.g. refractive surgery or transplantation), or infection of the cornea with viruses, bacteria, or other infectious agents, may initiate an inflammatory reaction mediated by the immune response and neovascularization (formation of new blood vessels). These processes may result in destructive cytopathic causes and may lead to thickening and opacification (clouding) of the cornea, which may ultimately lead to a reduction of visual clarity and sometimes sight.

Trauma of the cornea (e.g., surgical or accidental) may lead to pain, inflammation, scarring, neovascularization, and/or discharge. Even in the absence of a particular infectious agent, corneal lesions can affect visual acuity and progress to further damage to the eye. Generally, corneal trauma may be typically treated with strong corticosteroids which may decrease inflammation. However, these agents may have severe secondary effects, including: 1) increased risk of infections (common in ocular trauma) by diminishing the protective immune response; 2) delayed healing of the cornea; 3) loss of an intact epithelial barrier; 4) increased ocular pressure; and 5) eventual deterioration of vision.

Globally, infection- and inflammation-associated eye diseases are the leading causes of corneal blindness and visual morbidity, with over 500 million individuals affected. Pathogen-associated ocular diseases are a complex combination of pathogen-mediated trauma and host-mediated pathologies, often with the most severe sequelae being a consequence of host inflammatory responses. Corneal infections are often treated with a combination of antimicrobials to eliminate pathogens and corticosteroids to reduce inflammation. However, several problems may arise from this approach.

First, effective antimicrobials are not always available for the infectious agents of the eye. For example, Adenoviral infections, which may cause epidemic outbreaks of highly contagious keratoconjunctivitis (pink eye) that can last up to a month, are not readily treatable by antimicrobials. Second, even when anti-viral medications are available and can kill the viruses, they cannot control the inflammatory response triggered by the infection. Typically, inflammation accounts for the clinical presentation of an ocular disease. Often the inflammatory response may cause secondary but more severe damage of the cornea. Third, many pathogens evolve drug resistance, which enables the pathogen to replicate even in the presence of the antimicrobial. For example, some strains of herpes simplex viruses (HSV), which are the leading cause of infectious corneal blindness in the United States, and Chlamydia trachomatis, a leading cause of infectious blindness worldwide, have developed drug resistant strains. Fourth, co-administration of steroids to suppress host anti-pathogen immune responses (inflammation) in infected individuals also blocks the protective role of the immune responses and enables uncontrolled replication, as well as pathogen-mediated disease progression.

Four herpes viruses are linked to severe infections of the eye that can result in blindness: HSV-1, HSV-2, VZV, and CMV. The National Eye Institute estimates that 450,000 Americans have experienced some form of ocular herpetic disease, with 50,000 new and recurrent cases diagnosed annually. Despite effective antivirals against HSV, approximately 25% of these cases develop serious inflammation-associated stromal keratitis. Individuals that have experienced ocular herpes have a 50% chance of recurrence with each repeated episode triggering deleterious CD4 and CD8 T cell responses that can result in scarring of the cornea and an eventual need for corneal transplantation. Although corneal transplantation restores the patient's sight, it does not cure the patient of his or her lifelong herpetic infection; therefore, recrudescence of infection in these individuals may renew the vicious cycle and result in damage to the implanted cornea.

Herpetic stromal keratitis (HSK), a blinding eye disease associated with HSV-1 infection, is not simply a virus-mediated disease of the corneal stroma, but a virus-associated chronic immuno-inflammatory disease of the eye. It is mediated by many complex immune mechanisms including macrophages, dendritic cells, T cells (Th1, Th2, T-regs and Th17), antibodies and even cytokines. Therefore, even with anti-herpetic drugs controlling HSV-1 replication, the vision threatening disease progresses through immune-mediated pathologies.

Clinical presentations of ocular diseases are a complex combination of trauma and host-mediated inflammation-associated pathologies that must be simultaneously controlled and resolved to prevent development of vision-threatening sequelae. Currently, no treatments exist that can effectively remedy all of these issues within the eye.

SUMMARY

In an embodiment of the present invention, a method of simultaneously inhibiting inflammation and neovascularization of corneal tissue of an eye and promoting healing of the eye is provided, including applying peg-Arginase I to the eye. The peg-Arginase I is applied exogenously. The eye may have been infected with an infectious agent. The infectious agent may be a virus. The peg-Arginase I may inhibit replication of the virus. The infectious agent may be a bacterium.

The eye may have been traumatized. The trauma may be from a medical procedure. The trauma may be from an accidental injury of the eye.

The peg-Arginase I may part of an ophthalmic formulation. The ophthalmic formulation may include peg-Arginase I and free peg molecules. The ophthalmic formulation may further include pH buffers. The ophthalmic formulation may be an eye drop. The eye may be a mammalian eye. The mammalian eye may be a human eye.

According to an embodiment of the present invention, a therapeutic method to treat an ocular disease is provided, including applying peg-Arginase I to an affected eye. The peg-Arginase I is part of an ophthalmic formulation. The affected eye may present at least one of inflammation and neovascularization. The ocular disease may be caused by an infectious agent. The infectious agent may be a virus. The peg-Arginase I may inhibit replication of the virus. The infectious agent may be a bacterium.

The ocular disease may be trauma to the affected eye. The trauma may be from a medical procedure. The ocular disease may be a corneal lesion.

According to an embodiment of the present invention, an anti-viral treatment is provided, including applying peg-Arginase I to a patient infected by a virus. The treatment may include administering free peg molecules with the peg-Arginase I to the patient. The peg-Arginase I may be part of an ophthalmic formulation. The ophthalmic formulation may include peg-Arginase I and free peg molecules. The peg-Arginase may be part of a respiratory inhalant formulation. The respiratory inhalant formulation may include peg-Arginase I and free peg molecules. Replication of the virus may be inhibited. The patient may be infected by at least one of HSV-1, HSV-2, CMV, VZV, Adenovirus and Influenza virus. The at least one of HSV-1, HSV-2, CMV, VZV, Adenovirus and Influenza virus may be drug resistant. The virus may have infected a respiratory system of the patient. The virus may have infected an ocular region of the patient.

According to an exemplary embodiment of the present invention, a method to promote healing of corneal trauma is provided, including applying peg-Arginase I to an affected eye. The trauma may be induced by at least one of accidental injury, surgical procedure, mechanical impact, and pathogenic infection.

According to an exemplary embodiment of the present invention, a method to treat ocular lesions is provided including applying peg-Arginase I to an affected eye. The peg-Arginase I is part of an ophthalmic formulation. The ophthalmic formulation may be comprised of peg-Arginase I and free peg molecules.

According to an exemplary embodiment of the present invention, a method to prevent ocular neovascularization is provided, including applying peg-Arginase I to an affected eye. The peg-Arginase I is part of an ophthalmic formulation. The ophthalmic formulation may be comprised of peg-Arginase I and free peg molecules.

According to an exemplary embodiment of the present invention, a method to prevent ocular inflammation is provided, including applying peg-Arginase I to an affected eye. The peg-Arginase I is part of an ophthalmic formulation. The ophthalmic formulation may be comprised of peg-Arginase I and free peg molecules.

DESCRIPTION OF DRAWINGS

FIG. 1A is a series of images of rabbit eyes with an 8 mm (area=200 mm²) region of cornea surgically debrided and treated with peg vehicle or peg-Arginase I, according to an example embodiment of the present invention.

FIG. 1B is a line graph showing areas of the corneal lesions over a period of six days, as represented by eyes in FIG. 1A.

FIG. 2 is a line graph showing combined ocular clinical scores over a period of six days, as represented by eyes in FIG. 1A.

FIG. 3 is a line graph showing corneal neovascularization over a period of six days, as represented by eyes in FIG. 1A.

FIG. 4 is a line graph showing scleral inflammation over a period of six days, as represented by eyes in FIG. 1A.

FIG. 5 is a bar graph showing infectious viral yield for cell cultures infected with HSV-1 and treated with a vehicle (peg vehicle), peg-Arginase I, or different concentrations of acyclovir, according to an example embodiment of the present invention.

FIG. 6 is a series of images showing virus-mediated cytopathic effects on cell cultures treated as described in FIG. 5.

FIG. 7A is a series of images of HSV-plaques showing capacity for cell-to-cell spread following treatment with a vehicle (peg vehicle), peg-Arginase I, or acyclovir, according to an example embodiment of the present invention.

FIG. 7B is a bar graph showing effects of treatment on cell-to-cell spread of HSV-1 for cultures treated as described in FIG. 7A.

FIG. 8A is a bar graph showing infectious HSV yield for cell cultures infected with an acyclovir resistant mutant HSV, according to an example embodiment of the present invention.

FIG. 8B is a bar graph showing infectious HSV yield for cell cultures infected with a different acyclovir resistant mutant HSV, according to an example embodiment of the present invention.

FIG. 9 is a bar graph showing replication of HSV-1 in primary corneal epithelial cell cultures treated with vehicle or peg-Arginase I, according to an example embodiment of the present invention.

FIG. 10 is line graph showing viral production in a rabbit eye model for eyes infected with HSV-1 and treated with controls (peg-BSA and PBS), 1% triflourothymidine, or peg-Arginase I, according to an example embodiment of the present invention.

FIG. 11 is a series of images of rabbit eyes infected with HSV-1 and treated with controls (peg-BSA or PBS), 1% triflourothymidine, or peg-Arginase I, according to an example embodiment of the present invention.

FIG. 12 is a line graph showing slit lamp examination scores over an 8 day period for the eyes shown in FIG. 11.

FIG. 13 is a line graph showing combined ocular clinical scores over an 8 day period for the eyes shown in FIG. 11.

FIG. 14 is a line graph showing corneal stromal inflammation over an 8 day period for the eyes shown in FIG. 11.

FIG. 15 is a line graph showing scleral inflammation over an 8 day period for the eyes shown in FIG. 11.

FIG. 16 is a line graph showing corneal neovascularization over an 8 day period for the eyes shown in FIG. 11.

FIG. 17 is a line graph showing corneal eyelid inflammation over an 8 day period for the eyes shown in FIG. 11.

FIG. 18 is a pair of images of cell cultures infected with Adenovirus and treated with control (peg-BSA) or peg-Arginase I drops, according to an example embodiment of the present invention.

FIG. 19 is a series of images of rabbit eyes with an Adenoviral infection and treated with control (peg-BSA), cidofovir, or peg-Arginase I drops, according to an example embodiment of the present invention.

FIG. 20 is a line graph showing slit lamp examination scores over an 8 day period for the eyes shown in FIG. 19.

FIG. 21 is a line graph showing combined ocular clinical scores over an 8 day period for the eyes shown in FIG. 19.

FIG. 22 is a line graph showing corneal neovascularization over an 8 day period for the eyes shown in FIG. 19.

FIG. 23 is a line graph showing scleral inflammation over an 8 day period for the eyes shown in FIG. 19.

FIG. 24 is a line graph showing corneal stromal inflammation over an 8 day period for the eyes shown in FIG. 19.

FIG. 25A is a series of images comparing effects of treatment with either control (peg-BSA) or peg-Arginase I on endothelial cell migration in a scratch wound healing model, according to an example embodiment of the present invention.

FIG. 25B is a bar graph showing a percentage of unhealed wound area after a twenty-four hour period for the wounds shown in FIG. 25A.

FIG. 26A is a pair of images of rabbit eyes having a VEGF pellet surgically implanted into a corneal micropocket and treated with vehicle or peg-Arginase I, according to an example embodiment of the present invention.

FIG. 26B is a bar graph showing areas of VEGF-mediated corneal neovascularization for the eyes shown in FIG. 26A

FIG. 27A is a series of images of a pair of rabbit eyes from the same rabbit showing clouding of the cornea in vehicle treated eyes, according to an example embodiment of the present invention.

FIG. 27B is a bar graph showing corneal cloudiness measurements for the eyes shown in FIG. 27A.

DESCRIPTION

Embodiments of the present disclosure provide a formulation of pegylated arginase I (peg-Arginase I) that simultaneously treats inflammatory reactions and neovascularization of corneal tissue, while promoting healing of a damaged cornea. Embodiments may include peg-Arginase I as part of an ophthalmic formulation, which may be applied topically to an affected eye. Embodiments of the present disclosure provide methods for improved treatment of ocular diseases whereby the methods simultaneously: (1) inhibit damaging inflammatory reactions without blocking protective host responses; (2) inhibit replication of multiple pathogens; (3) prevent neovascularization processes; and (4) promote healing. Further, embodiments of the present disclosure target pathways that are unlikely to lead to the evolution of drug resistance and may be effective against current drug resistant pathogens.

Embodiments of the present disclosure include methods of modulating amino acid concentrations in microenvironments. Embodiments of the present disclosure modulate amino acid concentrations as a therapeutic approach for viral infections. In certain embodiments, amino acid concentrations are modulated to inhibit viral replication and prevent deleterious inflammation. In embodiments of the present invention, peg-Arginase I is administered as an antiviral. Embodiments of the present invention may be utilized to treat a broad range of viral infections. In certain embodiments of the present disclosure, peg-Arginase I may be administered to a patient infected by a virus. Peg-Arginase I may be administered to deplete arginine in a recipient. Depletion of arginine may inhibit viral replication and/or inflammatory responses.

Arginase is a manganese-containing enzyme and is part of the urea cycle. In most mammals, two isozymes of arginase exist: (1) arginase I, which functions in the urea cycle and is located primarily in the cytoplasm of the liver, and (2) arginase II, which may regulate arginine/ornithine concentrations in the cell. Pegylation is the process of covalent attachment of polyethylene glycol (peg) polymer chains to another molecule such as a drug or protein. Pegylation may mask an agent from a host's immune system and may provide increased solubility, mobility and longevity to the agent. peg-Arginase I is a formulation of arginase I that has been pegylated.

In embodiments of the present invention, application of peg-Arginase I may occur exogenously and may be delivered as a topical ophthalmic formulation such as an eye drop. This peg-Arginase I ophthalmic eye drop may be composed of both protein conjugated and free peg molecules which may facilitate enzyme stability and mask the peg-Arginase I from host responses. Presence of free peg molecules may also impart properties to the formulation that aid in peg-Arginase I's ophthalmic activities. The peg-Arginase I eye drop may contain various buffer systems that maintain a pH level that is conducive for Arginase enzymatic activity and is tolerated by the eye. In certain embodiments, peg-Arginase I may be applied in combination with other antivirals, anti-inflammatories or anti-inflammatory treatments. peg-Arginase I application is effective in treating corneal trauma, promoting healing of the cornea, and preventing deleterious vision-threatening inflammation.

Embodiments of the present disclosure may be affective against both RNA and DNA viral infections, including both enveloped and non-enveloped viruses. Embodiments of the present disclosure may be used to treat a variety of viral infections, including but not limited to, ocular infections and respiratory infections. Embodiments of the present disclosure may be administered orally or as an inhalant formulation. Embodiments of the present disclosure may be incorporated into an injection composition.

Embodiments of the present disclosure may also be used to treat certain bacterial infections, including Chlamydia trachomatis. The present disclosure may be utilized to treat a variety of pathogen and inflammation-associated ocular diseases, including: Adenovirus-associated epidemic keratoconjunctivitis (no current effective treatment); herpes simplex-associated eye infections; varicella zoster-associated eye infections; herpes stromal keratitis; inflammation-associated diseases; CMV retinitis; and drug resistant pathogens. Moreover, embodiments may be used to treat humans or in various veterinarian applications, including feline, canine, and equine ocular diseases. The foregoing list is exemplary only and is not intended to identify all ocular diseases that may be treated with the methods identified herein.

In an exemplary embodiment, the present disclosure may be employed to treat ocular lesions, which may be caused by accidental or surgical trauma. Application of peg-Arginase I to a corneal lesion accelerates wound healing while reducing or eliminating ocular inflammation, neovascularization and inflammatory discharge. FIGS. 1 through 4 and Tables 1 through 5 demonstrate experimental results of an embodiment of the present disclosure whereby surgically-induced corneal lesions were treated with peg-Arginase I. FIG. 1A shows representative images of the lesions and demonstrates that treatment with an embodiment of the present invention accelerated healing of the lesion compared to peg-vehicle treatments. As shown in FIG. 1B and Tables 1 and 2, rates of corneal healing and injury closure were substantially faster when treated with an embodiment of the present invention, with 100% of eyes reaching clinical cure for epithelial defects two days faster than those treated only with peg-vehicle.

TABLE 1 Calculated Times of Corneal Epithelium Closure % Closure peg-ArgI Vehicle 25% 14 h 36 h 50% 30 h 48 h 75% 38 h 64 h

TABLE 2 Number of Eyes Clinically Cured for Area of Corneal Debridement Number Eyes Number Eyes Clinically Cured Clinically Cured DAY (peg-ArgI) (Vehicle) 0 0/5 0/5 1 0/5 0/5 2 0/5 0/5 3 3/5 (60%) 1/5 (20%) 4 5/5 (100%) 2/5 (40%) 6 5/5 (100%) 5/5 (100%)

Moreover, as shown in FIG. 2 and Table 3, peg-Arginase I treated eyes did not experience an increase in presentation of any clinical symptoms, and combined clinical presentations markedly declined with treatment. On day four, 80% of eyes treated with an embodiment of the present invention exhibited no symptomology from the surgically-induced trauma with all eyes clinically cured by day six. In contrast, only 40% of vehicle treated eyes showed clinical cure for all ocular parameters by day six of treatment.

TABLE 3 Number of Eyes Clinically Cured of All Combined Ocular Clinical Conditions Number Eyes Number Eyes Clinically Cured Clinically Cured DAY (peg-ArgI) (Vehicle) 0 0/5 0/5 1 0/5 0/5 2 0/5 0/5 3 0/5 0/5 4 4/5 (80%) 0/5 6 5/5 (100%) 2/5 (40%)

FIGS. 3 and 4, as well as Tables 4 and 5, illustrate that treatment with an embodiment of the present invention prevents corneal neovascularization and inflammation of the sclera in this corneal wound healing model. These results not only demonstrate effectiveness of the present invention for treating traumatic ocular issues, but exemplify that embodiments of the ophthalmic formulation are well-tolerated in the eye even in the presence of traumatic damage.

TABLE 4 Number of Eyes Clinically Cured of Corneal Neovascularization Number Eyes Number Eyes Clinically Cured Clinically Cured DAY (peg-ArgI) (Vehicle) 0 5/5 (100%) 5/5 (100%) 1 5/5 (100%) 0/5 2 5/5 (100%) 0/5 3 5/5 (100%) 0/5 4 5/5 (100%) 0/5 6 5/5 (100%) 3/5 (60%)

TABLE 5 Number of Eyes Clinically Cured of Scleral Inflammation (Injection) Number Eyes Number Eyes Clinically Cured Clinically Cured DAY (peg-ArgI) (Vehicle) 0 5/5 (100%) 5/5 (100%) 1 5/5 (100%) 1/5 (20%) 2 5/5 (100%) 1/5 (20%) 3 5/5 (100%) 4/5 (80)% 4 5/5 (100%) 4/5 (80) 6 5/5 (100%) 5/5 (100%)

Accordingly, embodiments of the present invention are effective in the treatment of ocular trauma, including reducing or eliminating inflammation, neovascularization and/or inflammatory discharge. Embodiments may substantially accelerate healing of the eye after an ocular trauma incident.

In another exemplary embodiment, the present disclosure may be employed to treat pathogenic infections of the eye (e.g., herpes simplex virus types 1 and 2 (HSV-1 and HSV-2) and Adenovirus infections). Embodiments may be used as a treatment against wild-type and/or drug resistant herpes simplex virus (HSV) replication and/or transmission, as well as HSV-mediated inflammation-associated ocular disease. In FIG. 5, cells infected by HSV-1 and treated with an embodiment of the present invention inhibited production of infectious virus by greater than 1000 fold even at high multiplicities of infection (MOIs). The present invention was at least as effective as high doses of a common anti-herpetic, acyclovir. As shown in FIGS. 6 and 7, peg-Arginase I treatment blocked virus-associated cytopathic effects, viral transmission to uninfected cells, and cell-to-cell spread. FIGS. 8A and 8B demonstrate that, for two different drug resistant mutant HSV viruses, peg-Arginase I is highly efficient at inhibiting drug-resistant viral replication, while anti-herpetic drugs, such as acyclovir, are not functional against such strains, even at high doses. FIG. 9 illustrates that antiviral effects of peg-Arginase I were also observed in primary human corneal epithelial cells, a cell line that recapitulates the natural cells where herpes viruses replicate within the eye.

In an in vivo rabbit eye model system, the ability of peg-Arginase I to prevent HSV-mediated inflammation-associated disease was assessed relative to a commonly prescribed ophthalmic antiviral-1% triflourothymidine (TFT). Rabbit eyes were infected with HSV, and infection and disease were allowed to establish prior to beginning treatment. FIG. 10 illustrates that at day three post infection production of viral titers were matched, and that upon treatment with peg-Arginase I, infectious viral titers were barely detectable. These results were better than that observed for treatment with the anti-herpetic 1% TFT. FIG. 11 depicts representative overall clinical presentation of ocular herpetic disease. In either of the control (PBS or peg-BSA) treatment groups, severe blinding disease was observed following infection, with presence of severe inflammatory discharge and blinding epithelial defects observed by slit lamp examination. In contrast, both peg-Arginase I and 1% TFT showed marked reduction in the presence of dendritic or geographic ulceration, and improved clinical appearance. The statistical significance of these clinical scores comparing between treatment groups is shown in Table 6 and indicates that five days of treatment with peg-Arginase I statistically improved clinical presentation of disease and resolved many inflammation and neovascularization associated clinical parameters.

TABLE 6 Significance of Clinical Scores Between Treatment Groups (P values; P > 0.05 = NS) Group Slit Lamp Combined Contrast Scleral Stromal Contrast Blepharitis Examination Examination Clinical Neovasc. Inflam. Inflam. Epithelium (Eyelid Infl.) peg-Arginase peg-BSA Start of Tx 1.0000 1.0000 1.0000 1.0000 1.0000 1.0000 0.9395 DAY 2 <0.0001 0.0032 <0.0001 <0.0001 0.0002 0.0003 0.0363 peg Argt vs PBS Start of Tx 1.0000 1.0000 1.0000 1.0000 1.0000 1.0000 1.0000 DAY 2 <0.0001 0.0088 0.0006 0.0049 0.0041 0.0426 0.0011 1% TFT vs PEG-DEA Start of Tx 1.0000 1.0000 1.0000 1.0000 1.0000 1.0000 0.9395 DAY 2 <0.0001 NS 0.0129 0.0012 0.0041 0.0129 NS 1% TFT vs PBS Start of Tx 1.0000 1.0000 0.9981 0.9999 1.0000 1.0000 1.0000 DAY 7 <0.0001 NS NS NS 0.0355 NS 0.0163 FIGS. 12 through 17 graphically depict assessment of the averages of these clinical parameters for each day throughout the duration of the experiment. Taken together, these results indicate that peg-Arginase I treatment not only prevents ocular replication of HSV, but can suppress and resolve virus-induced inflammation-associated disease and thwart vision-threatening vascularization of the cornea.

In another exemplary embodiment, the present disclosure may be employed to treat other inflammation-associated ocular diseases, such as those induced by Adenovirus infection. Clinical presentation following Adenoviral infection of the eye may proceed even when antiviral compounds, such as cidofovir, are present. Clinical presentation of Adenovirus-associated ocular disease may be due to uncontrolled inflammatory responses to the infection even following viral clearance. FIG. 18 illustrates that peg-Arginase I prevents Adenovirus-mediated cellular cytopathic effects and exhibits no toxicity to cells.

In an in vivo rabbit eye model system, the ability of peg-Arginase I to prevent inflammation-associated disease following Adenoviral infection was examined. Rabbit eyes were infected with Adenovirus and eight hours later treatment was initiated. Eyes were treated four times daily with 10 U peg-Arginase I per 50 μl dose. FIG. 19 depicts representative images from the Adenovirus Type 5 “pink-eye” clinical disease rabbit eye model showing that peg-Arginase I treated eyes showed fewer clinical symptoms, including less corneal vascularization, epiphora, blepharitis, and scleral injection, compared to eyes treated with peg-BSA control or the potent antiviral cidofovir. FIGS. 20 through 24 illustrate that peg-Arginase I suppresses clinical presentation of disease at all treatment days, including suppression of ocular inflammation and neovascularization. These effects were independent of its ability to inhibit Adenoviral replication, since the antiviral cidofovir did not prevent clinical disease presentation. These properties of peg-Arginase I illustrate the present invention's utility in preventing numerous vision-threatening ocular diseases that present clinically as inflammation or neovascularization of the eye.

In another exemplary embodiment, the present disclosure may be employed to prevent and resolve corneal neovascularization and vascularization-associated edema. As observed in all other model systems, peg-Arginase I treatment prevented and/or reduced presentation of vascularization of the cornea, a vision-threatening condition that is associated with many ocular diseases. A key mediator and initiator of corneal vascularization may be vascular endothelial growth factor (VEGF). FIGS. 25A and 25B illustrate that peg-Arginase I prevents VEGF-mediated migration of primary vascular endothelial cells, a prerequisite for blood vessel growth and expansion onto the cornea.

In an in vivo rabbit eye model system, the ability of peg-Arginase I to prevent VEGF-mediated corneal vascularization was assessed by implanting slow release VEGF pellets within a corneal micropocket 3 mm from the corneal limbus. Eyes were subsequently treated with either peg-Arginase I (right, OD eye) or peg-BSA vehicle control (left, OS eye) 4 times daily at a dose of 10 U per 50 μl drop. FIGS. 26A and 26B demonstrate that the extent and areas of neovascularization of the cornea were significantly reduced in peg-Arginase I treated eyes compared to peg-BSA treated controls. Moreover, even when vascularization was present, FIGS. 27A and 27B establish that peg-Arginase I treatment prevented the appearance of corneal edema that resulted in corneal clouding and epithelial defects. As shown, peg-Arginase I inhibits vision-threatening corneal vascularization, further enabling peg-Arginase I to prevent and ameliorate vision-threatening aspects of many ocular diseases. Moreover, inhibition of vascularization assists in suppressing deleterious inflammatory responses.

Although certain embodiments discussed herein address ocular challenge models, embodiments of the present disclosure inhibit viral replication, neovascularization, and inflammatory responses without limitation to the location of the viral infection. Embodiments of the present disclosure may be utilized to treat a variety of viral infections regardless of whether the infection is within a patient's eyes.

While the embodiments are described with reference to various implementations and exploitations, it will be understood that these embodiments are illustrative and that the scope of the inventions is not limited to them. Many variations, modifications, additions, and improvements are possible. Further still, any steps described herein may be carried out in any desired order, and any desired steps may be added or deleted. The specification and drawings are accordingly to be regarded in an illustrative rather than in a restrictive sense. 

What is claimed is:
 1. An anti-viral treatment, comprising: administering peg-Arginase I to a patient infected with a virus.
 2. The treatment of claim 1, further comprising: administering free peg molecules with the peg-Arginase I to the patient.
 3. The treatment of claim 1, wherein the peg-Arginase I is part of an ophthalmic formulation.
 4. The treatment of claim 3, wherein the ophthalmic formulation comprises peg-Arginase I and free peg molecules.
 5. The treatment of claim 1, wherein the peg-Arginase is part of a respiratory inhalant formulation.
 6. The treatment of claim 5, wherein the respiratory inhalant formulation comprises peg-Arginase I and free peg molecules.
 7. The treatment of claim 1, wherein replication of the virus is inhibited.
 8. The treatment of claim 1, wherein the patient is infected by at least one of HSV-1, HSV-2, CMV, VZV, Adenovirus, and Influenza virus.
 9. The treatment of claim 8, wherein the at least one of HSV-1, HSV-2, CMV, VZV, Adenovirus, and Influenza virus is drug resistant.
 10. The treatment of claim 1, wherein the peg-Arginase I is administered along with at least one other anti-viral compound.
 11. The treatment of claim 1, wherein the virus has infected a respiratory system of the patient.
 12. The treatment of claim 1, wherein the virus has infected an ocular region of the patient. 